Myanmar FDA registration 8171394536ea2375bbf49d70020cbe75
Omnilink Elite Peripheral Stent System
Device classification
- Brand Name
- Abbott
Registration information
- Analysis ID
- 8171394536ea2375bbf49d70020cbe75
- Registration Date
- April 18, 2022
Manufacturer
- Name
- Abbott Vascular
Authorized Representative
About this record
Access comprehensive regulatory information for Omnilink Elite Peripheral Stent System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8171394536ea2375bbf49d70020cbe75 and manufactured by Abbott Vascular. The device was registered on April 18, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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